Camptodactyly Of Toe Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Camptodactyly is a painless flexion contracture of the proximal interphalangeal (PIP) joint that is usually gradually progressive. This term refers to camptodactyly of one or more toes. (Human Phenotype Ontology, HP_0001836)
External Link	https://www.disgenet.org/browser/0/1/0/C4021774
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Genes

9 genes associated with the disease Camptodactyly Of Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
CHRNG	cholinergic receptor, nicotinic, gamma (muscle)
FBN2	fibrillin 2
FGFR3	fibroblast growth factor receptor 3
FHL1	four and a half LIM domains 1
FLNA	filamin A, alpha
MMP2	matrix metallopeptidase 2
PHF6	PHD finger protein 6
PIEZO2	piezo-type mechanosensitive ion channel component 2
SCARF2	scavenger receptor class F, member 2